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A NEW CLASS OF CYP2C9 INHIBITORS: PROBING 2C9 SPECIFICITY WITH HIGH-AFFINITY BENZBROMARONE DERIVATIVES

Charles W. Locuson II, Jan L. Wahlstrom, Denise A. Rock, Dan A. Rock and Jeffrey P. Jones
Drug Metabolism and Disposition July 2003, 31 (7) 967-971; DOI: https://doi.org/10.1124/dmd.31.7.967

Article Information

vol. 31 no. 7 967-971
DOI 
https://doi.org/10.1124/dmd.31.7.967
PubMed 
12814975
Published By 
American Society for Pharmacology and Experimental Therapeutics
Print ISSN 
0090-9556
Online ISSN 
1521-009X
History 
  • Received February 24, 2003
  • Accepted March 19, 2003
  • Published online July 1, 2003.
Copyright & Usage 
The American Society for Pharmacology and Experimental Therapeutics

Author Information

  1. Charles W. Locuson II,
  2. Jan L. Wahlstrom,
  3. Denise A. Rock,
  4. Dan A. Rock and
  5. Jeffrey P. Jones
  1. Washington State University, School of Molecular Biosciences (C.W.L. II) and Department of Chemistry (De.A.R., Da.A.R., J.P.J.), Pullman, Washington; and Camitro Corp., Redwood City, California (J.L.W.)
  1. Address correspondence to:
    Jeffrey P. Jones, Washington State University, Department of Chemistry, Pullman, WA 99164-4630. E-mail: jpj{at}wsu.edu
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OtherAccelerated Communication

A NEW CLASS OF CYP2C9 INHIBITORS: PROBING 2C9 SPECIFICITY WITH HIGH-AFFINITY BENZBROMARONE DERIVATIVES

Charles W. Locuson, Jan L. Wahlstrom, Denise A. Rock, Dan A. Rock and Jeffrey P. Jones
Drug Metabolism and Disposition July 1, 2003, 31 (7) 967-971; DOI: https://doi.org/10.1124/dmd.31.7.967
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